تفاعل #42612

ord-81b48af23f104facb77c3ddc8f18f085

المتفاعلات

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was then heated under agitation
  2. 2
    درجة الحرارةto reflux for 16 hours
  3. 3
    أخرىThe reaction solution was then evaporated to dryness
  4. 4
    أخرىThe mixture was separated
  5. 5
    استخلاصthe aqueous phase was extracted twice with ethyl acetate
  6. 6
    غسيلwashed with water and brine
  7. 7
    تركيزThe resulting yellow solution was concentrated to ˜50 ml
  8. 8
    أخرىto precipitate out
  9. 9
    ترشيحThe solid was filtered off
  10. 10
    غسيلwashed with ethanol and diethyl ether
  11. 11
    أخرىThe mother liquor was then evaporated to dryness
  12. 12
    تركيزconcentrated to ˜50 ml
  13. 13
    أخرىAn off-white solid precipitated out
  14. 14
    درجة الحرارةThe mixture was cooled in an ice bath
  15. 15
    ترشيحthe solid was filtered off
  16. 16
    غسيلwashed with ethanol and diethyl ether

الإجراء التجريبي

To a 250 ml 3-neck round bottom flask was added (20 g, 0.3332 moles) urea, (150 ml) ethanol and (42.42 g, 0.2175 moles, 0.65 eq) ethylbromopyruvate. The mixture was then heated under agitation to reflux for 16 hours. The reaction solution changed from yellow to red in color. The reaction solution was then evaporated to dryness and the crude product was taken up in (50 ml) water and (150 ml) ethyl acetate. The pH was adjusted from 1 to 10 using 2N sodium hydroxide, changing the biphasic mixture a dark red. The mixture was separated and the aqueous phase was extracted twice with ethyl acetate. The organic layers were then combined and washed with water and brine. The resulting yellow solution was concentrated to ˜50 ml, causing an off-white solid to precipitate out. The solid was filtered off and washed with ethanol and diethyl ether. The mother liquor was then evaporated to dryness and the resulting oily solid was taken up in (150 ml) ethyl acetate and concentrated to ˜50 ml. An off-white solid precipitated out. The mixture was cooled in an ice bath, and the solid was filtered off and washed with ethanol and diethyl ether to give ethyl 2-amino-1,3-oxazole-4-carboxylate (14.79 g).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07727997B2uspto-grants-2010_06